FDA Inspection 924841 — Owen Mumfordltd.

Owen Mumfordltd. — FEI 3000191104

The FDA completed an inspection of Owen Mumfordltd. on March 26, 2015 in Oxford. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 26, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Oxford (United Kingdom)